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Medical Device Project Manager Jobs in Atlanta, GA

CorDx

Regulatory Affairs Manager (Atlanta)

Atlanta, GA · On-site

Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements. * Strong organizational and project management skills with the ability to manage ...

CorDx

Regulatory Affairs Manager (Atlanta)

Atlanta, GA · On-site

Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements. * Strong organizational and project management skills with the ability to manage ...

CorDx

Regulatory Affairs Manager (Atlanta)

Atlanta, GA · On-site

Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements. * Strong organizational and project management skills with the ability to manage ...

Spectrum Plastics Group

Product Manager

Alpharetta, GA · On-site

Solid knowledge of medical device regulatory frameworks and quality standards . * Highly analytical with the ability to translate market data into actionable strategies. * Strong project management ...

SPECTRUM PLASTICS MASTER

Product Manager

Alpharetta, GA · On-site

Solid knowledge of medical device regulatory frameworks and quality standards . * Highly analytical with the ability to translate market data into actionable strategies. * Strong project management ...

CorDx

Office Manager/Administrative Manager

Atlanta, GA · On-site

Within a biotechnology and medical device environment, the Office Manager / Administrative Manager ... Support executive leadership with administrative projects, scheduling, meeting coordination, travel ...

CorDx

Office Manager/Administrative Manager

Atlanta, GA · On-site

Within a biotechnology and medical device environment, the Office Manager / Administrative Manager ... Support executive leadership with administrative projects, scheduling, meeting coordination, travel ...

CorDx

Office Manager/Administrative Manager

Atlanta, GA · On-site

Within a biotechnology and medical device environment, the Office Manager / Administrative Manager ... Support executive leadership with administrative projects, scheduling, meeting coordination, travel ...

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All JobsMedical Device Project JobsMedical Device Project Manager JobsMedical Device Project Manager Jobs in Atlanta, GA

Medical Device Project Manager information

See Atlanta, GA salary details

$37K

$98.7K

$155.8K

How much do medical device project manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for medical device project manager in Atlanta, GA is $98,745.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $118,300.00 per year, depending on experience, location, and employer.

What is a medical device project manager?

A Medical Device Project Manager oversees the planning, development, and launch of medical devices, ensuring compliance with regulatory standards. They coordinate cross-functional teams, manage timelines, budgets, and risks, and facilitate communication between stakeholders. Their role involves working closely with engineering, regulatory, quality, and marketing teams to bring safe and effective medical devices to market.

What are the day-to-day responsibilities of a medical device project manager?

As a Medical Device Project Manager, your daily duties typically include coordinating the activities of cross-functional teams—such as engineering, quality assurance, regulatory affairs, and marketing—to ensure project milestones are met. You'll oversee timelines, budgets, and documentation, while also addressing risks, facilitating communication, and managing stakeholder expectations. Regular tasks might involve leading project meetings, updating project trackers, monitoring regulatory compliance, and troubleshooting challenges that arise throughout the product development lifecycle. Successful project managers balance strategic planning with hands-on problem solving to keep complex medical device projects moving smoothly toward launch.

What are the key skills and qualifications needed to thrive in a medical device project manager position, and why are they important?

To thrive as a Medical Device Project Manager, you need a strong knowledge of medical device development, regulatory compliance, and project management, often supported by a background in engineering or life sciences and certifications like PMP or Six Sigma. Familiarity with tools such as Microsoft Project, quality management systems (QMS), and regulatory submission platforms (such as FDA eSubmitter) is highly valuable. Excellent leadership, problem-solving skills, and effective communication are essential for coordinating cross-functional teams and navigating complex project demands. These skills are crucial for delivering compliant, high-quality medical devices on time and within budget while ensuring collaboration across technical and clinical stakeholders.

What are popular job titles related to Medical Device Project Manager jobs in Atlanta, GA?

For Medical Device Project Manager jobs in Atlanta, GA, the most frequently searched job titles are:

What job categories do people searching Medical Device Project Manager jobs in Atlanta, GA look for?

The top searched job categories for Medical Device Project Manager jobs in Atlanta, GA are:

Medical Device Project Manager jobs near you
Infographic showing various Medical Device Project Manager job openings in Atlanta, GA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $98,745 per year, or $47.5 per hour.

Regulatory Affairs Manager (Atlanta)

CorDx

Atlanta, GA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 28 days ago

Job description

Who is CorDx  
 

CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.  
 

Job Type: Full time  
Job Title: Regulatory Affairs Manager
Location: Onsite - Atlanta, GA

Position Summary:

The Regulatory Affairs Manager will support the preparation, review, and submission of regulatory documentation for medical device products, ensuring compliance with applicable regulatory requirements including FDA, ISO 13485, and other global standards. This position collaborates with cross-functional teams to provide regulatory input during product development and throughout the product lifecycle, helping to secure timely product approvals and regulatory clearances.

Key Responsibilities:

  • Prepare, review, and coordinate the submission of regulatory documents including 510(k), technical files, and other filings to regulatory agencies.
  • Ensure product compliance with FDA regulations, ISO 13485, and applicable international standards.
  • Provide regulatory support to product development teams by offering guidance on applicable regulations and documentation requirements.
  • Stay current on changes in regulatory requirements and assist in assessing the impact on company processes and products.
  • Perform regulatory assessments for product changes and propose appropriate regulatory pathways.
  • Maintain documentation and records of all regulatory submissions and correspondence.
  • Support the preparation for regulatory agency meetings, audits, and inspections.
  • Collaborate with internal departments such as R&D, Quality, and Operations to ensure regulatory deliverables are met in a timely manner.

Requirements

Education:

  • Bachelor's degree in Regulatory Affairs, Life Sciences, Engineering, or a related field required.
  • Master's degree preferred.

Professional Experience:

  • 5-7 years of regulatory affairs experience within the medical device or IVD industry.
  • Working knowledge of 510(k) submissions and regulatory documentation processes.
  • Experience interacting with FDA and other regulatory agencies preferred.

Skills & Competencies:

  • Solid understanding of FDA regulations (21 CFR Part 820), ISO 13485, and medical device regulatory requirements.
  • Strong organizational and project management skills with the ability to manage multiple projects and priorities.
  • Excellent communication, problem-solving, and attention to detail.
  • Ability to work collaboratively in cross-functional teams and manage document workflows.

Benefits

  • Highly competitive compensation package.
  • Comprehensive medical, dental, and vision insurance.
  • 401(k) plan with generous company contributions.
  • Flexible paid time off (PTO) policy.
  • Additional substantial benefits.

Equal Opportunity Statement: We are an equal opportunity employer committed to inclusion and diversity. We do not discriminate based on race, gender, religion, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any other protected characteristic.

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